Toluene → 3-Chloro-5-methoxyphenol

HRID 272728

반응식

HRID 272728 반응식
[Cl:1][C:2]1[CH:7]=[C:6]([O:8][CH3:9])[CH:5]=[C:4]([O:10]C)[CH:3]=1.B(Br)(Br)Br.C1(C)C=CC=CC=1>C(Cl)Cl>[Cl:1][C:2]1[CH:3]=[C:4]([OH:10])[CH:5]=[C:6]([O:8][CH3:9])[CH:7]=1

참가 물질

5

반응 조건

온도
-78 °C

실험 절차

1-Chloro-3,5-dimethoxy-benzene (1.72 g, 10 mmol) in 10 mL of CH2Cl2 was cooled to −78° C., followed by 1.0 M BBr3 in toluene (10 mL, 10 mmol) added dropwise. The solution was stirred at −78° C. for 1 hour, and then allowed to warmed to room temperature over 2 hours. The reaction was quenched with water, and the aqueous layer was extracted with additional CH2Cl2. The combined organic layers were washed with brine, dried, and concentrated under pressure. The residue was purified by silica gel column chromatography eluting with 1:1 EtOAc/Hexanes to give 0.51 g of the title compound. MS (APCI) m/e 159 (M+H)+, 1H NMR (500 MHz, DMSO-d6): □ 9.88 (s, 1H), 6.43 (m, 1H), 6.39 (m, 1H), 6.28 (m, 1H), 3.70 (s, 3H).

후처리

  1. additionadded dropwise
  2. temperatureallowed to warmed to room temperature over 2 hours
  3. customThe reaction was quenched with water
  4. extractionthe aqueous layer was extracted with additional CH2Cl2
  5. washThe combined organic layers were washed with brine
  6. customdried
  7. concentrationconcentrated under pressure
  8. customThe residue was purified by silica gel column chromatography
  9. washeluting with 1:1 EtOAc/Hexanes

출처 및 근거

ORD 기록
ord-5b6fa880f6dd4232b7b7109137d830c8
출처 데이터셋
uspto-grants-2008_11
특허 번호
US07456169B2

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